Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8702 |
| ensemblid | ENSG00000121578.13 |
| hgncid | 927 |
| symbol | B4GALT4 |
| name | beta-1,4-galactosyltransferase 4 |
| refseq_nuc | NM_003778.4 |
| refseq_prot | NP_003769.1 |
| ensembl_nuc | ENST00000393765.7 |
| ensembl_prot | ENSP00000377360.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 119211742 |
| end | 119240878 |
| strand | - |
| ver | v1.2 |
| region | chr3:119211742-119240878 |
| region5000 | chr3:119206742-119245878 |
| regionname0 | B4GALT4_chr3_119211742_119240878 |
| regionname5000 | B4GALT4_chr3_119206742_119245878 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 344 | 295 | 66 | 53 | 134 | 15 | 25 | 107 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | MGFNL others(339): Show |
chr3 | 119206742 | 119245878 |
| a0002 | 0/0 | 344 | 138 | 27 | 23 | 72 | 1 | 15 | 57 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | MGFNL others(339): Show |
chr3 | 119206742 | 119245878 |
| a0003 | 0/0 | 344 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | MGFNL others(339): Show |
chr3 | 119206742 | 119245878 |
| a0004 | 0/0 | 344 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | MGFNL others(339): Show |
chr3 | 119206742 | 119245878 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1032 | 206 | 58 | 36 | 81 | 10 | 19 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | ATGGG others(1027): Show |
chr3 | 119206742 | 119245878 | ||
| a0001c0003 | 0/0 | 1032 | 82 | 1 | 17 | 53 | 5 | 6 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | ATGGG others(1027): Show |
chr3 | 119206742 | 119245878 | ||
| a0001c0004 | 0/0 | 1032 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | ATGGG others(1027): Show |
chr3 | 119206742 | 119245878 | ||
| a0001c0005 | 0/0 | 1032 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | ATGGG others(1027): Show |
chr3 | 119206742 | 119245878 | ||
| a0001c0009 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | ATGGG others(1027): Show |
chr3 | 119206742 | 119245878 | ||
| a0002c0002 | 0/0 | 1032 | 137 | 27 | 23 | 71 | 1 | 15 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | ATGGG others(1027): Show |
chr3 | 119206742 | 119245878 | ||
| a0002c0008 | 0/0 | 1032 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | ATGGG others(1027): Show |
chr3 | 119206742 | 119245878 | ||
| a0003c0006 | 0/0 | 1032 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | ATGGG others(1027): Show |
chr3 | 119206742 | 119245878 | ||
| a0004c0007 | 0/0 | 1032 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | ATGGG others(1027): Show |
chr3 | 119206742 | 119245878 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2234 | 79 | 26 | 9 | 41 | 0 | 3 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0001t0002 | 0/1 | 2234 | 41 | 5 | 7 | 17 | 2 | 9 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0001t0003 | 0/0 | 2234 | 70 | 16 | 16 | 23 | 8 | 7 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0001t0007 | 1/0 | 2234 | 8 | 5 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0001t0009 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0001t0012 | 0/0 | 2234 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0001t0013 | 0/0 | 2234 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0001t0014 | 0/0 | 2234 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0001t0018 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0003t0001 | 0/0 | 2234 | 4 | 1 | 0 | 3 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0003t0002 | 0/0 | 2234 | 74 | 0 | 17 | 46 | 5 | 6 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0003t0009 | 0/0 | 2234 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0003t0016 | 0/0 | 2234 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0003t0020 | 0/0 | 2234 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGG others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0004t0001 | 0/0 | 2234 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0005t0010 | 0/0 | 2234 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0001c0009t0002 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0002c0002t0001 | 0/0 | 2234 | 68 | 1 | 7 | 55 | 1 | 4 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0002c0002t0004 | 0/0 | 2234 | 35 | 7 | 3 | 16 | 0 | 9 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0002c0002t0005 | 0/0 | 2234 | 13 | 0 | 11 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0002c0002t0006 | 0/0 | 2234 | 8 | 7 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0002c0002t0008 | 0/0 | 2234 | 5 | 5 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0002c0002t0009 | 0/0 | 2234 | 2 | 1 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0002c0002t0011 | 0/0 | 2234 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0002c0002t0015 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0002c0002t0017 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0002c0002t0019 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0002c0008t0001 | 0/0 | 2234 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0003c0006t0002 | 0/0 | 2234 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| a0004c0007t0006 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | AGTGC others(2229): Show |
chr3 | 119206742 | 119245878 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0009 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0014 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0007 | 0/0 | 8 | 0 | 1 | 4 | 0 | 3 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0026 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0003 | 0/0 | 16 | 0 | 6 | 4 | 4 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0018 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0007g0011 | 1/0 | 7 | 4 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0013g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0014g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0001t0018g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0001 | 0/0 | 38 | 0 | 15 | 16 | 4 | 3 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0019 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0009g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0016g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0003t0020g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0004t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0005t0010g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0005t0010g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0001c0009t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0002 | 0/0 | 28 | 0 | 2 | 25 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0004 | 0/0 | 14 | 0 | 1 | 6 | 0 | 7 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0005g0012 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0005g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0005g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0006g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0008g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0009g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0011g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0011g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0015g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0017g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0002t0019g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0002c0008t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0003c0006t0002g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| a0004c0007t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0075 | EUR | GBR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0156 | EUR | GBR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | GBR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0154 | EUR | FIN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0001 | EUR | FIN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00423 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00423 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00639 | hp2 | a0002 | c0002 | t0004 | g0020 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00642 | hp1 | a0001 | c0001 | t0013 | g0042 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00673 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00733 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00735 | hp1 | a0002 | c0002 | t0005 | g0012 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG00741 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01069 | hp2 | a0001 | c0003 | t0002 | g0019 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01070 | hp2 | a0002 | c0002 | t0005 | g0012 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01074 | hp1 | a0002 | c0002 | t0005 | g0074 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01081 | hp1 | a0002 | c0002 | t0005 | g0063 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01081 | hp2 | a0002 | c0002 | t0005 | g0012 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01106 | hp1 | a0002 | c0002 | t0006 | g0069 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01109 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01167 | hp2 | a0001 | c0001 | t0013 | g0042 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | PUR | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0083 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0047 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01358 | hp2 | a0002 | c0002 | t0005 | g0089 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01361 | hp2 | a0002 | c0002 | t0005 | g0012 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0001 | EUR | IBS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01516 | hp1 | a0001 | c0003 | t0002 | g0019 | EUR | IBS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0026 | EUR | IBS | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01884 | hp1 | a0002 | c0002 | t0008 | g0027 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0088 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01891 | hp2 | a0002 | c0002 | t0015 | g0116 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01934 | hp2 | a0002 | c0002 | t0005 | g0021 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0079 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01943 | hp2 | a0002 | c0002 | t0005 | g0021 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01952 | hp2 | a0002 | c0002 | t0004 | g0190 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01975 | hp2 | a0002 | c0002 | t0004 | g0004 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01978 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01978 | hp2 | a0002 | c0002 | t0005 | g0021 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01993 | hp1 | a0002 | c0002 | t0005 | g0062 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01993 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02055 | hp1 | a0001 | c0001 | t0014 | g0046 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0128 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0212 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02080 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02129 | hp2 | a0001 | c0003 | t0001 | g0038 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02145 | hp1 | a0002 | c0002 | t0004 | g0113 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02148 | hp2 | a0002 | c0002 | t0009 | g0149 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0209 | EAS | CDX | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | CDX | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02165 | hp2 | a0001 | c0003 | t0016 | g0205 | EAS | CDX | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02257 | hp1 | a0001 | c0001 | t0018 | g0072 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02257 | hp2 | a0002 | c0002 | t0006 | g0034 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02258 | hp1 | a0001 | c0001 | t0012 | g0131 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0001 | AMR | PEL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02451 | hp2 | a0002 | c0002 | t0011 | g0045 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0031 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02615 | hp2 | a0002 | c0002 | t0004 | g0077 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02622 | hp1 | a0002 | c0002 | t0008 | g0095 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02622 | hp2 | a0002 | c0002 | t0011 | g0167 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02630 | hp2 | a0002 | c0002 | t0006 | g0070 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02647 | hp2 | a0002 | c0002 | t0006 | g0064 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02698 | hp1 | a0001 | c0003 | t0002 | g0001 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02698 | hp2 | a0002 | c0002 | t0004 | g0004 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0031 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02723 | hp1 | a0002 | c0002 | t0019 | g0179 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0188 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0059 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0146 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02738 | hp2 | a0002 | c0002 | t0004 | g0004 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02886 | hp1 | a0002 | c0002 | t0011 | g0045 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02896 | hp1 | a0002 | c0002 | t0008 | g0027 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02897 | hp2 | a0002 | c0002 | t0008 | g0027 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02976 | hp1 | a0002 | c0002 | t0004 | g0196 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03017 | hp2 | a0002 | c0002 | t0004 | g0185 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03041 | hp2 | a0001 | c0005 | t0010 | g0035 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03098 | hp2 | a0002 | c0002 | t0004 | g0194 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03195 | hp1 | a0004 | c0007 | t0006 | g0127 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0163 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03209 | hp2 | a0001 | c0005 | t0010 | g0035 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03225 | hp2 | a0002 | c0002 | t0009 | g0148 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03239 | hp2 | a0001 | c0003 | t0002 | g0001 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03486 | hp2 | a0002 | c0002 | t0006 | g0065 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03491 | hp1 | a0002 | c0002 | t0004 | g0004 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03491 | hp2 | a0003 | c0006 | t0002 | g0053 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03492 | hp2 | a0002 | c0002 | t0004 | g0004 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03516 | hp1 | a0002 | c0002 | t0004 | g0071 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03540 | hp2 | a0002 | c0002 | t0006 | g0068 | AFR | GWD | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03579 | hp1 | a0002 | c0002 | t0006 | g0034 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03654 | hp2 | a0002 | c0002 | t0005 | g0012 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03669 | hp2 | a0003 | c0006 | t0002 | g0053 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03704 | hp2 | a0002 | c0002 | t0004 | g0004 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03831 | hp1 | a0002 | c0002 | t0004 | g0004 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0184 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0204 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0151 | SAS | BEB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG04199 | hp1 | a0002 | c0002 | t0005 | g0012 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG04204 | hp1 | a0001 | c0003 | t0002 | g0206 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG04204 | hp2 | a0002 | c0002 | t0004 | g0191 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0001 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | STU | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18522 | hp1 | a0001 | c0005 | t0010 | g0054 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18747 | hp1 | a0002 | c0002 | t0004 | g0016 | EAS | CHB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18747 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | CHB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18906 | hp2 | a0002 | c0002 | t0017 | g0193 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18943 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18944 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18945 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18946 | hp1 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0058 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18950 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18953 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18953 | hp2 | a0001 | c0003 | t0002 | g0049 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18954 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18959 | hp1 | a0002 | c0002 | t0004 | g0182 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18966 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18967 | hp2 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18969 | hp2 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0211 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18975 | hp1 | a0001 | c0003 | t0002 | g0213 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18975 | hp2 | a0002 | c0008 | t0001 | g0084 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18978 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18979 | hp1 | a0001 | c0003 | t0002 | g0208 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18980 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18982 | hp2 | a0002 | c0002 | t0004 | g0048 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18988 | hp2 | a0002 | c0002 | t0004 | g0197 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18989 | hp1 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18991 | hp2 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18993 | hp1 | a0001 | c0003 | t0002 | g0203 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18995 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18995 | hp2 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18997 | hp2 | a0001 | c0003 | t0002 | g0199 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18999 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19003 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19006 | hp1 | a0001 | c0003 | t0020 | g0221 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19009 | hp1 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19009 | hp2 | a0001 | c0003 | t0002 | g0198 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19011 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19012 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0046 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19058 | hp2 | a0002 | c0002 | t0004 | g0186 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19063 | hp2 | a0002 | c0002 | t0004 | g0048 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19064 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19066 | hp2 | a0001 | c0003 | t0002 | g0202 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19067 | hp2 | a0001 | c0003 | t0002 | g0200 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19074 | hp2 | a0001 | c0003 | t0009 | g0178 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19075 | hp2 | a0001 | c0003 | t0002 | g0214 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19078 | hp1 | a0001 | c0003 | t0002 | g0207 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19080 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19084 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19086 | hp1 | a0001 | c0003 | t0002 | g0049 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19088 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19090 | hp2 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19091 | hp1 | a0001 | c0003 | t0009 | g0215 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19240 | hp1 | a0001 | c0009 | t0002 | g0093 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA19240 | hp2 | a0002 | c0002 | t0004 | g0020 | AFR | YRI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ASW | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0157 | EUR | TSI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0001 | EUR | TSI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0216 | EUR | TSI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0001 | EUR | TSI | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA20905 | hp1 | a0002 | c0002 | t0004 | g0004 | SAS | GIH | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0082 | SAS | GIH | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0187 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02486 | hp1 | a0002 | c0002 | t0008 | g0132 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG02559 | hp2 | a0002 | c0002 | t0004 | g0020 | AFR | ACB | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | MSL | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18955 | hp1 | a0002 | c0002 | t0004 | g0004 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA18955 | hp2 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | USA | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA20300 | hp2 | a0002 | c0002 | t0006 | g0066 | AFR | USA | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | LWK | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0120 | REF | REF | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0011 | REF | REF | B4GALT4_chr3_119206742_119245878 | B4GALT4 | chr3 | 119206742 | 119245878 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:119212554 | C | A | 1 | a0003 | 2 | HG03491.hp2 HG03669.hp2 |
missense_variant | MODERATE | c.1030G>T | p.Ala344Ser | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 1422/2234 | 1030/1035 | 344/344 | chr3 | 119212554 | |||
| chr3:119212556 | C | T | 1 | a0004 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1028G>A | p.Gly343Asp | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 1420/2234 | 1028/1035 | 343/344 | chr3 | 119212556 | |||
| chr3:119226949 | G | C | 2 | a0002 a0004 |
139 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
missense_variant | MODERATE | c.346C>G | p.Gln116Glu | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/8 | 738/2234 | 346/1035 | 116/344 | chr3 | 119226949 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:119224213 | G | A | 1 | a0001c0004 | 3 | HG01884.hp2 HG02572.hp2 HG02717.hp2 |
synonymous_variant | LOW | c.519C>T | p.Leu173Leu | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/8 | 911/2234 | 519/1035 | 173/344 | chr3 | 119224213 | |||
| chr3:119229848 | G | A | 1 | a0002c0008 | 1 | NA18975.hp2 | splice_region_variant&synonymous_variant | LOW | c.252C>T | p.Leu84Leu | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/8 | 644/2234 | 252/1035 | 84/344 | chr3 | 119229848 | |||
| chr3:119229869 | G | A | 2 | a0001c0003 a0001c0009 |
83 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
synonymous_variant | LOW | c.231C>T | p.Cys77Cys | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/8 | 623/2234 | 231/1035 | 77/344 | chr3 | 119229869 | |||
| chr3:119229998 | G | A | 2 | a0001c0005 a0001c0009 |
4 | HG03041.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
synonymous_variant | LOW | c.102C>T | p.Phe34Phe | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/8 | 494/2234 | 102/1035 | 34/344 | chr3 | 119229998 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:119211797 | T | C | 1 | a0001c0003t0016 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 752 | chr3 | 119211797 | ||||||
| chr3:119211896 | T | A | 1 | a0002c0002t0017 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*653A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 653 | chr3 | 119211896 | ||||||
| chr3:119211944 | G | C | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0013 others(7): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*605C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 605 | chr3 | 119211944 | ||||||
| chr3:119211962 | A | G | 4 | a0001c0001t0018 a0002c0002t0006 a0002c0002t0011 others(1): Show |
13 | HG01106.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*587T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 587 | chr3 | 119211962 | ||||||
| chr3:119211980 | G | A | 2 | a0002c0002t0005 a0002c0002t0015 |
14 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*569C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 569 | chr3 | 119211980 | ||||||
| chr3:119212037 | G | A | 9 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0006 others(6): Show |
68 | HG00423.hp2 HG00639.hp2 HG00735.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*512C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 512 | chr3 | 119212037 | ||||||
| chr3:119212055 | T | C | 1 | a0001c0001t0018 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 494 | chr3 | 119212055 | ||||||
| chr3:119212266 | C | T | 3 | a0002c0002t0005 a0002c0002t0008 a0002c0002t0015 |
19 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*283G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 283 | chr3 | 119212266 | ||||||
| chr3:119212438 | C | A | 1 | a0001c0001t0013 | 2 | HG00642.hp1 HG01167.hp2 |
3_prime_UTR_variant | MODIFIER | c.*111G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 111 | chr3 | 119212438 | ||||||
| chr3:119212474 | C | T | 1 | a0001c0001t0012 | 2 | HG02109.hp1 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*75G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 75 | chr3 | 119212474 | ||||||
| chr3:119212542 | C | T | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(20): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
3_prime_UTR_variant | MODIFIER | c.*7G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 8/8 | 7 | chr3 | 119212542 | ||||||
| chr3:119230131 | C | A | 1 | a0001c0005t0010 | 3 | HG03041.hp2 HG03209.hp2 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-32G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/8 | 32 | chr3 | 119230131 | ||||||
| chr3:119230184 | G | A | 1 | a0001c0001t0014 | 2 | HG02055.hp1 NA19043.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-85C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/8 | chr3 | 119230184 | |||||||
| chr3:119236988 | C | T | 1 | a0002c0002t0015 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-281G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/8 | 6889 | chr3 | 119236988 | ||||||
| chr3:119237006 | T | C | 1 | a0001c0005t0010 | 3 | HG03041.hp2 HG03209.hp2 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-299A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/8 | 6907 | chr3 | 119237006 | ||||||
| chr3:119237041 | G | A | 8 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0013 others(5): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-334C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/8 | chr3 | 119237041 | |||||||
| chr3:119240874 | G | C | 1 | a0001c0003t0020 | 1 | NA19006.hp1 | 5_prime_UTR_variant | MODIFIER | c.-388C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/8 | 10775 | chr3 | 119240874 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:119212694 | A | G | 1 | a0002c0002t0001g0075 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.903-13T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119212694 | |||||||
| chr3:119212822 | G | T | 218 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(215): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.903-141C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119212822 | |||||||
| chr3:119213188 | G | T | 6 | a0002c0002t0006g0066 a0002c0002t0006g0068 a0002c0002t0006g0069 others(3): Show |
7 | HG01106.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.903-507C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213188 | |||||||
| chr3:119213240 | G | A | 1 | a0001c0001t0003g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.903-559C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213240 | |||||||
| chr3:119213280 | G | A | 2 | a0001c0001t0003g0153 a0001c0001t0003g0159 |
2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.903-599C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213280 | |||||||
| chr3:119213338 | C | T | 1 | a0001c0001t0018g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.903-657G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213338 | |||||||
| chr3:119213354 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.903-673A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213354 | |||||||
| chr3:119213601 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(8): Show |
28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.903-920A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213601 | |||||||
| chr3:119213980 | T | G | 2 | a0002c0002t0001g0114 a0002c0002t0009g0148 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.903-1299A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119213980 | |||||||
| chr3:119214022 | A | G | 198 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(195): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.903-1341T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214022 | |||||||
| chr3:119214061 | C | CA | 10 | a0002c0002t0006g0034 a0002c0002t0006g0064 a0002c0002t0006g0065 others(7): Show |
12 | HG01106.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.903-1381dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214061 | |||||||
| chr3:119214068 | TAAA | T | 18 | a0001c0005t0010g0054 a0002c0002t0004g0004 a0002c0002t0004g0016 others(15): Show |
38 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(35): Show |
intron_variant | MODIFIER | c.903-1390_903-1388d others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214068 | |||||||
| chr3:119214106 | G | T | 2 | a0002c0002t0001g0114 a0002c0002t0009g0148 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.903-1425C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214106 | |||||||
| chr3:119214140 | T | C | 28 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(25): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.903-1459A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214140 | |||||||
| chr3:119214221 | A | G | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.903-1540T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214221 | |||||||
| chr3:119214483 | A | G | 1 | a0001c0003t0002g0207 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.902+1757T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214483 | |||||||
| chr3:119214494 | G | A | 1 | a0001c0003t0002g0051 | 2 | NA18989.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.902+1746C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214494 | |||||||
| chr3:119214512 | G | T | 1 | a0002c0002t0006g0064 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.902+1728C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214512 | |||||||
| chr3:119214517 | C | T | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.902+1723G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214517 | |||||||
| chr3:119214719 | T | G | 1 | a0002c0002t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.902+1521A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214719 | |||||||
| chr3:119214720 | G | T | 1 | a0002c0002t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.902+1520C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214720 | |||||||
| chr3:119214800 | C | T | 1 | a0001c0001t0003g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.902+1440G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214800 | |||||||
| chr3:119214900 | A | G | 4 | a0001c0001t0003g0018 a0001c0001t0003g0041 a0001c0001t0003g0144 others(1): Show |
8 | HG00639.hp1 HG01123.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.902+1340T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214900 | |||||||
| chr3:119214905 | G | A | 1 | a0001c0001t0001g0024 | 3 | HG02809.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.902+1335C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119214905 | |||||||
| chr3:119215228 | G | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0094 |
4 | HG02809.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.902+1012C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215228 | |||||||
| chr3:119215381 | A | G | 198 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(195): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.902+859T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215381 | |||||||
| chr3:119215454 | C | A | 1 | a0001c0003t0002g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.902+786G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215454 | |||||||
| chr3:119215703 | T | C | 1 | a0001c0001t0003g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.902+537A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215703 | |||||||
| chr3:119215752 | G | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG03130.hp1 HG03209.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.902+488C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215752 | |||||||
| chr3:119215777 | T | A | 1 | a0002c0002t0004g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.902+463A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119215777 | |||||||
| chr3:119216167 | G | A | 2 | a0002c0002t0006g0066 a0002c0002t0006g0069 |
2 | HG01106.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.902+73C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119216167 | |||||||
| chr3:119216183 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.902+57A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119216183 | |||||||
| chr3:119216214 | G | A | 1 | a0002c0002t0008g0095 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.902+26C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 7/7 | chr3 | 119216214 | |||||||
| chr3:119216369 | T | A | 23 | a0001c0001t0002g0103 a0001c0001t0002g0189 a0001c0001t0003g0044 others(20): Show |
55 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.798-25A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216369 | |||||||
| chr3:119216429 | TACACACA others(11): Show |
T | 1 | a0002c0002t0001g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.798-103_798-86delG others(17): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216429 | |||||||
| chr3:119216431 | C | T | 29 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(26): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.798-87G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216431 | |||||||
| chr3:119216431 | CACACACA others(7): Show |
C | 4 | a0002c0002t0001g0006 a0002c0002t0008g0027 a0002c0002t0008g0095 others(1): Show |
6 | HG01884.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.798-101_798-88delA others(13): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216431 | |||||||
| chr3:119216433 | CACACACG others(5): Show |
C | 36 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(33): Show |
78 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.798-101_798-90delA others(11): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216433 | |||||||
| chr3:119216435 | CACACGCA others(3): Show |
C | 20 | a0001c0001t0001g0096 a0002c0002t0004g0004 a0002c0002t0004g0016 others(17): Show |
38 | HG00423.hp2 HG00639.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.798-101_798-92delA others(9): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216435 | |||||||
| chr3:119216437 | CACGCACA others(1): Show |
C | 151 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(148): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.798-101_798-94delA others(7): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216437 | |||||||
| chr3:119216439 | CGCACAT | C | 7 | a0001c0001t0001g0098 a0001c0001t0003g0018 a0001c0001t0003g0041 others(4): Show |
11 | HG00639.hp1 HG01123.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.798-101_798-96delA others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216439 | |||||||
| chr3:119216445 | TACACACA others(1): Show |
T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0094 |
4 | HG02809.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.798-109_798-102del others(8): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216445 | |||||||
| chr3:119216449 | C | T | 1 | a0002c0002t0001g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.798-105G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216449 | |||||||
| chr3:119216451 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0003g0018 a0001c0001t0003g0041 others(2): Show |
9 | HG00639.hp1 HG01123.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.798-107G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216451 | |||||||
| chr3:119216453 | C | T | 144 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(141): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.798-109G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216453 | |||||||
| chr3:119216455 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.798-111G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216455 | |||||||
| chr3:119216558 | C | T | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.798-214G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216558 | |||||||
| chr3:119216565 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.798-221G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119216565 | |||||||
| chr3:119217002 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.798-658G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217002 | |||||||
| chr3:119217003 | G | A | 1 | a0002c0002t0004g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.798-659C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217003 | |||||||
| chr3:119217152 | A | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(65): Show |
140 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.798-808T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217152 | |||||||
| chr3:119217176 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0094 |
4 | HG02809.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.798-832T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217176 | |||||||
| chr3:119217225 | A | G | 218 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(215): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.798-881T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217225 | |||||||
| chr3:119217294 | C | CT | 28 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(25): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.798-951dupA | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217294 | |||||||
| chr3:119217367 | C | T | 2 | a0002c0002t0001g0114 a0002c0002t0009g0148 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.798-1023G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217367 | |||||||
| chr3:119217454 | A | T | 28 | a0001c0001t0002g0201 a0001c0003t0002g0001 a0001c0003t0002g0008 others(25): Show |
80 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.798-1110T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217454 | |||||||
| chr3:119217479 | C | A | 28 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(25): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.798-1135G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217479 | |||||||
| chr3:119217495 | C | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
60 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(57): Show |
intron_variant | MODIFIER | c.798-1151G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217495 | |||||||
| chr3:119217497 | A | G | 1 | a0001c0001t0003g0151 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.797+1153T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217497 | |||||||
| chr3:119217516 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.797+1134G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217516 | |||||||
| chr3:119217544 | A | G | 20 | a0002c0002t0005g0012 a0002c0002t0005g0021 a0002c0002t0005g0062 others(17): Show |
31 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.797+1106T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217544 | |||||||
| chr3:119217643 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.797+1007A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217643 | |||||||
| chr3:119217659 | G | C | 1 | a0001c0009t0002g0093 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.797+991C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217659 | |||||||
| chr3:119217716 | G | A | 2 | a0001c0001t0003g0168 a0001c0001t0014g0046 |
3 | HG02055.hp1 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.797+934C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217716 | |||||||
| chr3:119217735 | C | T | 3 | a0002c0002t0001g0114 a0002c0002t0004g0071 a0002c0002t0009g0148 |
3 | HG02258.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.797+915G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217735 | |||||||
| chr3:119217784 | G | A | 1 | a0001c0001t0002g0026 | 3 | HG00140.hp2 HG00642.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.797+866C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217784 | |||||||
| chr3:119217792 | G | A | 1 | a0001c0001t0003g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.797+858C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217792 | |||||||
| chr3:119217828 | G | A | 28 | a0001c0001t0002g0201 a0001c0003t0002g0001 a0001c0003t0002g0008 others(25): Show |
80 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.797+822C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217828 | |||||||
| chr3:119217842 | CA | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(60): Show |
145 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.797+807delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217842 | |||||||
| chr3:119217842 | CAA | C | 97 | a0001c0001t0001g0107 a0001c0001t0001g0138 a0001c0001t0002g0007 others(94): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.797+806_797+807del others(2): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217842 | |||||||
| chr3:119217842 | CAAAAA | C | 25 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(22): Show |
65 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.797+803_797+807del others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217842 | |||||||
| chr3:119217861 | A | G | 10 | a0002c0002t0005g0012 a0002c0002t0005g0021 a0002c0002t0005g0062 others(7): Show |
19 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.797+789T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119217861 | |||||||
| chr3:119218167 | C | T | 218 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(215): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.797+483G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218167 | |||||||
| chr3:119218178 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.797+472C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218178 | |||||||
| chr3:119218194 | G | A | 2 | a0001c0001t0003g0029 a0001c0001t0003g0142 |
4 | HG00544.hp1 HG02132.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.797+456C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218194 | |||||||
| chr3:119218280 | T | C | 10 | a0002c0002t0006g0034 a0002c0002t0006g0064 a0002c0002t0006g0065 others(7): Show |
12 | HG01106.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.797+370A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218280 | |||||||
| chr3:119218490 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0092 a0001c0001t0001g0133 others(3): Show |
10 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.797+160C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218490 | |||||||
| chr3:119218606 | C | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0002c0002t0001g0114 |
5 | HG02258.hp2 HG02809.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.797+44G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 6/7 | chr3 | 119218606 | |||||||
| chr3:119218919 | C | T | 3 | a0002c0002t0004g0016 a0002c0002t0004g0182 a0002c0002t0004g0197 |
7 | HG00423.hp2 NA18747.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.675-147G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119218919 | |||||||
| chr3:119219198 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0094 |
4 | HG02809.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.675-426A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219198 | |||||||
| chr3:119219272 | T | C | 81 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(78): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.675-500A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219272 | |||||||
| chr3:119219470 | A | T | 1 | a0001c0001t0003g0150 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.675-698T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219470 | |||||||
| chr3:119219643 | A | T | 1 | a0001c0001t0003g0043 | 2 | NA18998.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.675-871T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219643 | |||||||
| chr3:119219727 | G | A | 2 | a0002c0002t0001g0059 a0002c0002t0001g0082 |
2 | HG02735.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.675-955C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219727 | |||||||
| chr3:119219769 | T | C | 3 | a0001c0004t0001g0031 a0001c0004t0001g0088 a0002c0002t0004g0194 |
4 | HG01884.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-997A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219769 | |||||||
| chr3:119219774 | A | G | 31 | a0001c0001t0002g0162 a0002c0002t0001g0002 a0002c0002t0001g0006 others(28): Show |
72 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.675-1002T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219774 | |||||||
| chr3:119219974 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.675-1202G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119219974 | |||||||
| chr3:119220175 | C | CA | 3 | a0001c0001t0003g0017 a0001c0003t0002g0184 a0002c0002t0004g0197 |
6 | HG03834.hp1 NA18986.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.675-1404dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220175 | |||||||
| chr3:119220256 | T | C | 1 | a0001c0009t0002g0093 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.675-1484A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220256 | |||||||
| chr3:119220386 | T | C | 1 | a0001c0003t0002g0208 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.675-1614A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220386 | |||||||
| chr3:119220421 | A | C | 1 | a0001c0001t0007g0188 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.675-1649T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220421 | |||||||
| chr3:119220439 | C | T | 3 | a0002c0002t0008g0027 a0002c0002t0008g0095 a0002c0002t0008g0132 |
5 | HG01884.hp1 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.675-1667G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220439 | |||||||
| chr3:119220440 | G | A | 1 | a0002c0002t0006g0070 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.675-1668C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220440 | |||||||
| chr3:119220442 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.675-1670C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220442 | |||||||
| chr3:119220533 | A | G | 31 | a0001c0001t0002g0162 a0002c0002t0001g0002 a0002c0002t0001g0006 others(28): Show |
72 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.675-1761T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220533 | |||||||
| chr3:119220632 | C | T | 4 | a0001c0003t0002g0050 a0001c0003t0002g0209 a0001c0003t0002g0211 others(1): Show |
5 | HG02080.hp1 HG02155.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.675-1860G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220632 | |||||||
| chr3:119220634 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.675-1862C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220634 | |||||||
| chr3:119220636 | C | T | 1 | a0001c0001t0003g0157 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.675-1864G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220636 | |||||||
| chr3:119220729 | G | T | 40 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
60 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(57): Show |
intron_variant | MODIFIER | c.675-1957C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220729 | |||||||
| chr3:119220761 | C | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
60 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(57): Show |
intron_variant | MODIFIER | c.675-1989G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220761 | |||||||
| chr3:119220765 | T | C | 2 | a0002c0002t0001g0023 a0002c0002t0001g0073 |
4 | NA18969.hp1 NA18980.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-1993A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220765 | |||||||
| chr3:119220782 | C | G | 1 | a0001c0001t0002g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.675-2010G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220782 | |||||||
| chr3:119220880 | G | A | 10 | a0002c0002t0005g0012 a0002c0002t0005g0021 a0002c0002t0005g0062 others(7): Show |
19 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.675-2108C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220880 | |||||||
| chr3:119220942 | C | T | 3 | a0001c0004t0001g0031 a0001c0004t0001g0088 a0002c0002t0004g0194 |
4 | HG01884.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-2170G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220942 | |||||||
| chr3:119220985 | C | CA | 29 | a0001c0001t0001g0130 a0001c0001t0002g0124 a0002c0002t0001g0002 others(26): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.675-2214dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119220985 | |||||||
| chr3:119221220 | T | C | 2 | a0001c0001t0003g0017 a0001c0003t0002g0184 |
5 | HG03834.hp1 NA18986.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.675-2448A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221220 | |||||||
| chr3:119221253 | G | A | 3 | a0001c0001t0002g0162 a0002c0002t0001g0114 a0002c0002t0009g0148 |
3 | HG02258.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.675-2481C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221253 | |||||||
| chr3:119221295 | T | G | 3 | a0001c0004t0001g0031 a0001c0004t0001g0088 a0002c0002t0004g0194 |
4 | HG01884.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-2523A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221295 | |||||||
| chr3:119221355 | A | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(8): Show |
28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.675-2583T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221355 | |||||||
| chr3:119221467 | C | T | 69 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0026 others(66): Show |
115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.674+2591G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221467 | |||||||
| chr3:119221536 | C | T | 16 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(13): Show |
36 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.674+2522G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221536 | |||||||
| chr3:119221553 | A | G | 67 | a0001c0001t0002g0162 a0002c0002t0001g0002 a0002c0002t0001g0006 others(64): Show |
139 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.674+2505T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221553 | |||||||
| chr3:119221564 | A | G | 2 | a0002c0002t0001g0078 a0002c0002t0001g0079 |
2 | HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.674+2494T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221564 | |||||||
| chr3:119221736 | C | A | 2 | a0001c0001t0003g0164 a0001c0001t0003g0165 |
2 | HG01099.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.674+2322G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221736 | |||||||
| chr3:119221782 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.674+2276G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221782 | |||||||
| chr3:119221834 | T | C | 1 | a0002c0002t0004g0048 | 2 | NA18982.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.674+2224A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221834 | |||||||
| chr3:119221914 | A | G | 1 | a0001c0001t0001g0024 | 3 | HG02809.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.674+2144T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119221914 | |||||||
| chr3:119222009 | G | C | 1 | a0001c0001t0018g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.674+2049C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222009 | |||||||
| chr3:119222056 | T | C | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.674+2002A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222056 | |||||||
| chr3:119222182 | T | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(38): Show |
61 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(58): Show |
intron_variant | MODIFIER | c.674+1876A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222182 | |||||||
| chr3:119222251 | G | A | 190 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(187): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.674+1807C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222251 | |||||||
| chr3:119222388 | A | G | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.674+1670T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222388 | |||||||
| chr3:119222419 | G | GGC | 80 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(77): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.674+1638_674+1639i others(4): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222419 | |||||||
| chr3:119222421 | A | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(77): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.674+1637T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222421 | |||||||
| chr3:119222422 | T | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(77): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.674+1636A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222422 | |||||||
| chr3:119222423 | C | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(77): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.674+1635G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222423 | |||||||
| chr3:119222428 | GC | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(77): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.674+1629delG | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222428 | |||||||
| chr3:119222525 | T | G | 1 | a0001c0001t0003g0172 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.674+1533A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222525 | |||||||
| chr3:119222540 | C | G | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.674+1518G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222540 | |||||||
| chr3:119222577 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.674+1481G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222577 | |||||||
| chr3:119222594 | A | G | 188 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(185): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.674+1464T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222594 | |||||||
| chr3:119222690 | T | C | 16 | a0002c0002t0005g0012 a0002c0002t0005g0021 a0002c0002t0005g0062 others(13): Show |
26 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.674+1368A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222690 | |||||||
| chr3:119222708 | T | G | 2 | a0001c0003t0009g0178 a0001c0003t0009g0215 |
2 | NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.674+1350A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222708 | |||||||
| chr3:119222787 | T | G | 9 | a0001c0001t0002g0026 a0001c0001t0002g0039 a0001c0001t0002g0101 others(6): Show |
12 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.674+1271A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222787 | |||||||
| chr3:119222845 | C | G | 7 | a0002c0002t0005g0012 a0002c0002t0005g0021 a0002c0002t0005g0062 others(4): Show |
14 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.674+1213G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222845 | |||||||
| chr3:119222895 | G | T | 190 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(187): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.674+1163C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222895 | |||||||
| chr3:119222902 | A | G | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.674+1156T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222902 | |||||||
| chr3:119222985 | A | G | 67 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(64): Show |
139 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.674+1073T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119222985 | |||||||
| chr3:119223040 | T | C | 1 | a0002c0002t0008g0132 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.674+1018A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223040 | |||||||
| chr3:119223045 | T | C | 31 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0025 others(28): Show |
46 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.674+1013A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223045 | |||||||
| chr3:119223289 | A | C | 2 | a0002c0002t0001g0114 a0002c0002t0009g0148 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.674+769T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223289 | |||||||
| chr3:119223378 | T | C | 28 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(25): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.674+680A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223378 | |||||||
| chr3:119223412 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(8): Show |
28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.674+646A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223412 | |||||||
| chr3:119223437 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.674+621C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223437 | |||||||
| chr3:119223628 | C | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.674+430G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223628 | |||||||
| chr3:119223697 | GC | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(77): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.674+360delG | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223697 | |||||||
| chr3:119223792 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.674+266C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223792 | |||||||
| chr3:119223862 | T | G | 9 | a0001c0001t0002g0026 a0001c0001t0002g0039 a0001c0001t0002g0101 others(6): Show |
12 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.674+196A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223862 | |||||||
| chr3:119223868 | G | A | 2 | a0002c0002t0001g0114 a0002c0002t0009g0148 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.674+190C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223868 | |||||||
| chr3:119223973 | G | A | 1 | a0001c0003t0002g0204 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.674+85C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223973 | |||||||
| chr3:119223974 | A | G | 1 | a0001c0003t0002g0204 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.674+84T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 5/7 | chr3 | 119223974 | |||||||
| chr3:119224307 | C | T | 1 | a0001c0003t0002g0203 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.487-62G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224307 | |||||||
| chr3:119224338 | T | C | 2 | a0001c0004t0001g0031 a0001c0004t0001g0088 |
3 | HG01884.hp2 HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.487-93A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224338 | |||||||
| chr3:119224372 | T | C | 1 | a0002c0002t0006g0034 | 2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.487-127A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224372 | |||||||
| chr3:119224387 | G | A | 28 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(25): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.487-142C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224387 | |||||||
| chr3:119224387 | G | C | 1 | a0001c0001t0003g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.487-142C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224387 | |||||||
| chr3:119224434 | T | A | 1 | a0001c0001t0003g0173 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.487-189A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224434 | |||||||
| chr3:119224454 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
4 | HG01255.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-209C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224454 | |||||||
| chr3:119224485 | C | G | 218 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(215): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.487-240G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224485 | |||||||
| chr3:119224557 | C | T | 7 | a0002c0002t0005g0012 a0002c0002t0005g0021 a0002c0002t0005g0062 others(4): Show |
14 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.487-312G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224557 | |||||||
| chr3:119224563 | T | G | 28 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(25): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.487-318A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224563 | |||||||
| chr3:119224595 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(8): Show |
28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.487-350A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224595 | |||||||
| chr3:119224638 | C | T | 1 | a0001c0003t0002g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.487-393G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224638 | |||||||
| chr3:119224705 | A | G | 187 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(184): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.487-460T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224705 | |||||||
| chr3:119224773 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(8): Show |
28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.487-528T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119224773 | |||||||
| chr3:119225052 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.487-807A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225052 | |||||||
| chr3:119225063 | A | G | 190 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(187): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.487-818T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225063 | |||||||
| chr3:119225302 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.487-1057A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225302 | |||||||
| chr3:119225428 | G | A | 3 | a0001c0003t0002g0209 a0001c0004t0001g0031 a0001c0004t0001g0088 |
4 | HG01884.hp2 HG02155.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-1183C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225428 | |||||||
| chr3:119225482 | C | T | 2 | a0002c0002t0001g0114 a0002c0002t0009g0148 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.487-1237G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225482 | |||||||
| chr3:119225563 | AT | A | 119 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0024 others(116): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.486+1245delA | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225563 | |||||||
| chr3:119225570 | T | G | 28 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(25): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.486+1239A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225570 | |||||||
| chr3:119225618 | A | G | 1 | a0001c0001t0002g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.486+1191T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225618 | |||||||
| chr3:119225648 | C | A | 28 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(25): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.486+1161G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225648 | |||||||
| chr3:119225649 | A | G | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.486+1160T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225649 | |||||||
| chr3:119225658 | T | A | 218 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(215): Show |
427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.486+1151A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225658 | |||||||
| chr3:119225777 | G | A | 1 | a0001c0001t0003g0156 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.486+1032C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225777 | |||||||
| chr3:119225897 | CTATA | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.486+908_486+911del others(4): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225897 | |||||||
| chr3:119225901 | A | G | 2 | a0002c0002t0008g0027 a0002c0002t0008g0132 |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.486+908T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225901 | |||||||
| chr3:119225986 | T | C | 1 | a0001c0001t0018g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.486+823A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225986 | |||||||
| chr3:119225990 | A | G | 1 | a0002c0002t0004g0185 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.486+819T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119225990 | |||||||
| chr3:119226103 | C | T | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.486+706G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226103 | |||||||
| chr3:119226123 | GA | G | 39 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0015 others(36): Show |
59 | HG00673.hp2 HG01109.hp1 HG01168.hp2 others(56): Show |
intron_variant | MODIFIER | c.486+685delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226123 | |||||||
| chr3:119226281 | G | A | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.486+528C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226281 | |||||||
| chr3:119226309 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486+500A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226309 | |||||||
| chr3:119226312 | T | C | 190 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(187): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.486+497A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226312 | |||||||
| chr3:119226498 | A | T | 1 | a0002c0002t0004g0190 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.486+311T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226498 | |||||||
| chr3:119226522 | C | T | 2 | a0002c0002t0001g0114 a0002c0002t0009g0148 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.486+287G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226522 | |||||||
| chr3:119226605 | A | G | 1 | a0001c0001t0002g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.486+204T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226605 | |||||||
| chr3:119226731 | T | C | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.486+78A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226731 | |||||||
| chr3:119226767 | G | A | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.486+42C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226767 | |||||||
| chr3:119226776 | C | G | 2 | a0001c0004t0001g0031 a0001c0004t0001g0088 |
3 | HG01884.hp2 HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.486+33G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 4/7 | chr3 | 119226776 | |||||||
| chr3:119227341 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.254-300C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227341 | |||||||
| chr3:119227354 | G | A | 1 | a0002c0002t0001g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.254-313C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227354 | |||||||
| chr3:119227476 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0129 others(6): Show |
14 | HG01433.hp2 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.254-435C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227476 | |||||||
| chr3:119227699 | T | C | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.254-658A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227699 | |||||||
| chr3:119227810 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.254-769C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227810 | |||||||
| chr3:119227839 | C | T | 2 | a0002c0002t0001g0114 a0002c0002t0009g0148 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.254-798G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227839 | |||||||
| chr3:119227904 | C | T | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.254-863G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227904 | |||||||
| chr3:119227909 | G | A | 1 | a0001c0001t0003g0155 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.254-868C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227909 | |||||||
| chr3:119227950 | G | A | 18 | a0001c0001t0003g0145 a0001c0001t0003g0161 a0002c0002t0005g0012 others(15): Show |
28 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.254-909C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227950 | |||||||
| chr3:119227982 | A | G | 28 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(25): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.254-941T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119227982 | |||||||
| chr3:119228206 | G | A | 1 | a0002c0002t0004g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.254-1165C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228206 | |||||||
| chr3:119228223 | C | T | 1 | a0001c0001t0018g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.254-1182G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228223 | |||||||
| chr3:119228284 | G | A | 2 | a0002c0002t0001g0083 a0002c0002t0001g0090 |
2 | HG01255.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.254-1243C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228284 | |||||||
| chr3:119228301 | C | A | 64 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0026 others(61): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.254-1260G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228301 | |||||||
| chr3:119228421 | T | C | 28 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(25): Show |
69 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.254-1380A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228421 | |||||||
| chr3:119228461 | T | C | 1 | a0001c0001t0018g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.253+1386A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228461 | |||||||
| chr3:119228499 | G | A | 2 | a0001c0001t0003g0168 a0001c0001t0014g0046 |
3 | HG02055.hp1 HG02809.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.253+1348C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228499 | |||||||
| chr3:119228791 | A | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1056T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228791 | |||||||
| chr3:119228792 | A | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1055T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228792 | |||||||
| chr3:119228793 | G | A | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1054C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228793 | |||||||
| chr3:119228794 | G | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1053C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228794 | |||||||
| chr3:119228795 | G | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1052C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228795 | |||||||
| chr3:119228797 | G | A | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1050C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228797 | |||||||
| chr3:119228798 | G | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1049C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228798 | |||||||
| chr3:119228799 | A | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1048T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228799 | |||||||
| chr3:119228800 | G | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1047C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228800 | |||||||
| chr3:119228804 | C | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1043G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228804 | |||||||
| chr3:119228805 | CAGG | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1039_253+1041d others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228805 | |||||||
| chr3:119228810 | G | A | 1 | a0001c0001t0003g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.253+1037C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228810 | |||||||
| chr3:119228810 | G | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1037C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228810 | |||||||
| chr3:119228811 | G | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1036C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228811 | |||||||
| chr3:119228812 | G | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1035C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228812 | |||||||
| chr3:119228813 | A | G | 4 | a0001c0001t0002g0013 a0001c0001t0002g0123 a0001c0001t0002g0124 others(1): Show |
8 | HG00609.hp2 HG02056.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.253+1034T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228813 | |||||||
| chr3:119228813 | A | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1034T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228813 | |||||||
| chr3:119228814 | T | A | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1033A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228814 | |||||||
| chr3:119228816 | A | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1031T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228816 | |||||||
| chr3:119228817 | A | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1030T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228817 | |||||||
| chr3:119228819 | G | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1028C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228819 | |||||||
| chr3:119228821 | A | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1026T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228821 | |||||||
| chr3:119228823 | T | TG | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1023_253+1024i others(3): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228823 | |||||||
| chr3:119228825 | A | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1022T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228825 | |||||||
| chr3:119228826 | TAAAAAG | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1015_253+1020d others(8): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228826 | |||||||
| chr3:119228833 | A | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1014T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228833 | |||||||
| chr3:119228834 | G | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1013C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228834 | |||||||
| chr3:119228836 | A | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1011T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228836 | |||||||
| chr3:119228837 | A | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1010T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228837 | |||||||
| chr3:119228838 | G | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1009C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228838 | |||||||
| chr3:119228839 | A | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1008T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228839 | |||||||
| chr3:119228840 | G | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1007C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228840 | |||||||
| chr3:119228841 | G | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1006C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228841 | |||||||
| chr3:119228843 | A | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1004T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228843 | |||||||
| chr3:119228844 | TGAG | T | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+1000_253+1002d others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228844 | |||||||
| chr3:119228848 | A | C | 17 | a0002c0002t0004g0004 a0002c0002t0004g0016 a0002c0002t0004g0020 others(14): Show |
37 | HG00423.hp2 HG00639.hp2 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.253+999T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228848 | |||||||
| chr3:119228921 | C | T | 10 | a0002c0002t0005g0012 a0002c0002t0005g0021 a0002c0002t0005g0062 others(7): Show |
19 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.253+926G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119228921 | |||||||
| chr3:119229028 | C | T | 1 | a0001c0001t0002g0210 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.253+819G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229028 | |||||||
| chr3:119229103 | C | T | 2 | a0002c0002t0001g0114 a0002c0002t0009g0148 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.253+744G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229103 | |||||||
| chr3:119229164 | C | T | 3 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0183 |
3 | HG02818.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.253+683G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229164 | |||||||
| chr3:119229308 | C | T | 200 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(197): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.253+539G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229308 | |||||||
| chr3:119229324 | A | G | 30 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(27): Show |
71 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.253+523T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229324 | |||||||
| chr3:119229409 | C | A | 75 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(72): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.253+438G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229409 | |||||||
| chr3:119229441 | C | T | 180 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(177): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.253+406G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229441 | |||||||
| chr3:119229590 | G | C | 7 | a0001c0001t0001g0195 a0002c0002t0004g0020 a0002c0002t0004g0071 others(4): Show |
9 | HG00639.hp2 HG01109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.253+257C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229590 | |||||||
| chr3:119229654 | C | A | 1 | a0002c0002t0005g0063 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.253+193G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229654 | |||||||
| chr3:119229771 | G | C | 44 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0002g0162 others(41): Show |
99 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.253+76C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 3/7 | chr3 | 119229771 | |||||||
| chr3:119230298 | G | A | 176 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(173): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-145-54C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230298 | |||||||
| chr3:119230333 | C | T | 1 | a0001c0001t0001g0024 | 3 | HG02809.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-145-89G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230333 | |||||||
| chr3:119230378 | T | C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG02965.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-145-134A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230378 | |||||||
| chr3:119230387 | C | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(8): Show |
28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.-145-143G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230387 | |||||||
| chr3:119230466 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-145-222G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230466 | |||||||
| chr3:119230500 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
15 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-145-256G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230500 | |||||||
| chr3:119230706 | G | C | 1 | a0002c0002t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-145-462C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230706 | |||||||
| chr3:119230719 | A | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0094 a0001c0001t0001g0115 others(8): Show |
15 | HG01433.hp2 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-145-475T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230719 | |||||||
| chr3:119230721 | A | G | 7 | a0002c0002t0004g0020 a0002c0002t0004g0071 a0002c0002t0004g0077 others(4): Show |
9 | HG00639.hp2 HG01106.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-145-477T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230721 | |||||||
| chr3:119230937 | G | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(8): Show |
28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.-145-693C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119230937 | |||||||
| chr3:119231165 | T | G | 2 | a0001c0005t0010g0035 a0001c0005t0010g0054 |
3 | HG03041.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-145-921A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231165 | |||||||
| chr3:119231263 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-145-1019C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231263 | |||||||
| chr3:119231333 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-145-1089C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231333 | |||||||
| chr3:119231398 | G | A | 1 | a0002c0002t0015g0116 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-145-1154C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231398 | |||||||
| chr3:119231441 | A | G | 37 | a0001c0001t0018g0072 a0002c0002t0001g0002 a0002c0002t0001g0006 others(34): Show |
86 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-145-1197T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231441 | |||||||
| chr3:119231652 | G | A | 57 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0036 others(54): Show |
117 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-145-1408C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231652 | |||||||
| chr3:119231658 | C | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(114): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.-145-1414G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231658 | |||||||
| chr3:119231667 | G | A | 1 | a0001c0001t0018g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-145-1423C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231667 | |||||||
| chr3:119231749 | T | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0115 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-145-1505A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231749 | |||||||
| chr3:119231750 | T | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0115 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-145-1506A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231750 | |||||||
| chr3:119231751 | T | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0115 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-145-1507A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231751 | |||||||
| chr3:119231762 | TTTTA | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
15 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-145-1522_-145-151 others(8): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231762 | |||||||
| chr3:119231791 | T | TTATAAAA | 140 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.-145-1554_-145-154 others(11): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231791 | |||||||
| chr3:119231801 | TA | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0129 others(4): Show |
11 | HG01433.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-145-1558delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231801 | |||||||
| chr3:119231804 | A | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0129 others(4): Show |
11 | HG01433.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-145-1560T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231804 | |||||||
| chr3:119231806 | T | TATAA | 27 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0022 others(24): Show |
68 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.-145-1563_-145-156 others(8): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231806 | |||||||
| chr3:119231807 | A | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0129 others(4): Show |
11 | HG01433.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-145-1563T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231807 | |||||||
| chr3:119231808 | A | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0129 others(4): Show |
11 | HG01433.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-145-1564T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119231808 | |||||||
| chr3:119232188 | A | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(12): Show |
24 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.-145-1944T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232188 | |||||||
| chr3:119232193 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-145-1949C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232193 | |||||||
| chr3:119232550 | T | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0129 others(5): Show |
12 | HG01433.hp2 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-145-2306A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232550 | |||||||
| chr3:119232551 | ATTCAGG | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0129 others(5): Show |
12 | HG01433.hp2 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-145-2313_-145-230 others(10): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232551 | |||||||
| chr3:119232561 | C | T | 1 | a0002c0002t0001g0076 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-145-2317G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232561 | |||||||
| chr3:119232568 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-145-2324C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232568 | |||||||
| chr3:119232714 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-145-2470A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232714 | |||||||
| chr3:119232864 | C | T | 2 | a0001c0001t0002g0162 a0001c0001t0002g0181 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-145-2620G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119232864 | |||||||
| chr3:119233098 | G | A | 49 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0092 others(46): Show |
101 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-145-2854C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233098 | |||||||
| chr3:119233131 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-145-2887C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233131 | |||||||
| chr3:119233169 | G | A | 27 | a0001c0001t0002g0201 a0001c0001t0002g0210 a0001c0003t0002g0001 others(24): Show |
78 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-145-2925C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233169 | |||||||
| chr3:119233246 | C | T | 1 | a0002c0002t0008g0095 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-145-3002G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233246 | |||||||
| chr3:119233307 | G | A | 1 | a0001c0001t0003g0156 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-145-3063C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233307 | |||||||
| chr3:119233397 | T | G | 1 | a0001c0001t0013g0042 | 2 | HG00642.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.-145-3153A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233397 | |||||||
| chr3:119233401 | C | T | 1 | a0002c0002t0001g0022 | 3 | NA18956.hp2 NA18968.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-145-3157G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233401 | |||||||
| chr3:119233600 | G | T | 1 | a0001c0001t0002g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-146+3253C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233600 | |||||||
| chr3:119233712 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0115 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-146+3141A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233712 | |||||||
| chr3:119233998 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(8): Show |
28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.-146+2855G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119233998 | |||||||
| chr3:119234081 | T | C | 31 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0094 others(28): Show |
51 | HG00609.hp2 HG00738.hp1 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.-146+2772A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234081 | |||||||
| chr3:119234116 | G | GTT | 11 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(8): Show |
20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-146+2735_-146+273 others(6): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234116 | |||||||
| chr3:119234221 | G | A | 2 | a0002c0002t0008g0027 a0002c0002t0008g0132 |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146+2632C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234221 | |||||||
| chr3:119234245 | G | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
12 | HG01168.hp2 HG01346.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-146+2608C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234245 | |||||||
| chr3:119234302 | T | C | 10 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(7): Show |
19 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.-146+2551A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234302 | |||||||
| chr3:119234328 | C | T | 1 | a0001c0004t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-146+2525G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234328 | |||||||
| chr3:119234364 | C | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(60): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-146+2489G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234364 | |||||||
| chr3:119234443 | C | A | 11 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(8): Show |
20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-146+2410G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234443 | |||||||
| chr3:119234459 | T | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0136 a0001c0001t0001g0137 others(6): Show |
12 | HG01168.hp2 HG01346.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-146+2394A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234459 | |||||||
| chr3:119234507 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-146+2346C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234507 | |||||||
| chr3:119234545 | T | C | 1 | a0001c0003t0002g0214 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-146+2308A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234545 | |||||||
| chr3:119234554 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-146+2299A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234554 | |||||||
| chr3:119234613 | A | G | 2 | a0001c0003t0001g0038 a0001c0003t0001g0110 |
3 | HG02129.hp2 NA18994.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-146+2240T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234613 | |||||||
| chr3:119234695 | G | A | 1 | a0001c0001t0003g0216 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-146+2158C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234695 | |||||||
| chr3:119234722 | G | A | 174 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(171): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-146+2131C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234722 | |||||||
| chr3:119234844 | C | T | 14 | a0001c0001t0001g0192 a0001c0001t0001g0195 a0002c0002t0004g0004 others(11): Show |
32 | HG00423.hp2 HG01109.hp1 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.-146+2009G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234844 | |||||||
| chr3:119234864 | C | T | 1 | a0002c0002t0001g0075 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-146+1989G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234864 | |||||||
| chr3:119234948 | G | A | 1 | a0002c0002t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-146+1905C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234948 | |||||||
| chr3:119234976 | T | C | 2 | a0001c0001t0002g0162 a0001c0001t0002g0181 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-146+1877A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119234976 | |||||||
| chr3:119235202 | T | G | 4 | a0002c0002t0005g0021 a0002c0002t0005g0063 a0002c0002t0005g0074 others(1): Show |
6 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-146+1651A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235202 | |||||||
| chr3:119235347 | T | C | 1 | a0001c0001t0002g0040 | 2 | NA18957.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-146+1506A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235347 | |||||||
| chr3:119235388 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-146+1465G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235388 | |||||||
| chr3:119235538 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-146+1315G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235538 | |||||||
| chr3:119235539 | T | C | 49 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0092 others(46): Show |
101 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-146+1314A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235539 | |||||||
| chr3:119235552 | A | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0036 others(17): Show |
31 | HG00438.hp2 HG00673.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.-146+1301T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235552 | |||||||
| chr3:119235596 | C | A | 52 | a0001c0001t0003g0003 a0001c0001t0003g0017 a0001c0001t0003g0018 others(49): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.-146+1257G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235596 | |||||||
| chr3:119235664 | C | G | 1 | a0001c0001t0003g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-146+1189G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235664 | |||||||
| chr3:119235925 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(9): Show |
29 | HG00408.hp1 HG01891.hp2 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.-146+928C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235925 | |||||||
| chr3:119235967 | GA | G | 2 | a0001c0003t0002g0008 a0001c0003t0002g0200 |
9 | NA18747.hp2 NA18941.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.-146+885delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119235967 | |||||||
| chr3:119236025 | G | A | 1 | a0002c0002t0005g0074 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-146+828C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236025 | |||||||
| chr3:119236084 | T | C | 174 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(171): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-146+769A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236084 | |||||||
| chr3:119236151 | A | G | 1 | a0001c0003t0002g0049 | 2 | NA18953.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-146+702T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236151 | |||||||
| chr3:119236156 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(8): Show |
28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.-146+697T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236156 | |||||||
| chr3:119236223 | A | C | 1 | a0001c0001t0001g0036 | 2 | HG01255.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-146+630T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236223 | |||||||
| chr3:119236224 | C | G | 1 | a0002c0002t0011g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-146+629G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236224 | |||||||
| chr3:119236254 | A | G | 11 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(8): Show |
20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-146+599T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236254 | |||||||
| chr3:119236311 | G | GA | 187 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0024 others(184): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-146+541dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236311 | |||||||
| chr3:119236406 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-146+447T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236406 | |||||||
| chr3:119236633 | C | T | 10 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(7): Show |
19 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.-146+220G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236633 | |||||||
| chr3:119236675 | A | G | 1 | a0001c0003t0002g0211 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-146+178T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236675 | |||||||
| chr3:119236764 | A | G | 201 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(198): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.-146+89T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236764 | |||||||
| chr3:119236796 | A | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0115 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-146+57T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 2/7 | chr3 | 119236796 | |||||||
| chr3:119237173 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-363-103A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237173 | |||||||
| chr3:119237208 | G | C | 2 | a0001c0001t0003g0157 a0001c0001t0003g0158 |
2 | HG01934.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-363-138C>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237208 | |||||||
| chr3:119237272 | C | CCTT | 101 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(98): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-363-205_-363-203d others(5): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237272 | |||||||
| chr3:119237406 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-363-336A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237406 | |||||||
| chr3:119237448 | G | A | 1 | a0001c0003t0002g0211 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-363-378C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237448 | |||||||
| chr3:119237559 | T | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0094 |
4 | HG02809.hp2 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-363-489A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237559 | |||||||
| chr3:119237594 | A | G | 4 | a0001c0001t0001g0067 a0001c0001t0001g0092 a0001c0004t0001g0031 others(1): Show |
5 | HG01891.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-363-524T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237594 | |||||||
| chr3:119237606 | C | T | 1 | a0002c0002t0015g0116 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-363-536G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237606 | |||||||
| chr3:119237659 | G | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
15 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-363-589C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237659 | |||||||
| chr3:119237932 | A | G | 49 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0092 others(46): Show |
101 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-363-862T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237932 | |||||||
| chr3:119237975 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-363-905T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119237975 | |||||||
| chr3:119238033 | G | A | 5 | a0001c0001t0001g0060 a0002c0002t0005g0021 a0002c0002t0005g0063 others(2): Show |
7 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.-363-963C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238033 | |||||||
| chr3:119238037 | C | T | 3 | a0002c0002t0006g0034 a0002c0002t0006g0064 a0002c0002t0006g0065 |
4 | HG02257.hp2 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-363-967G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238037 | |||||||
| chr3:119238053 | G | A | 1 | a0002c0002t0008g0095 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-363-983C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238053 | |||||||
| chr3:119238171 | G | A | 1 | a0002c0002t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-363-1101C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238171 | |||||||
| chr3:119238263 | T | TA | 82 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0002g0007 others(79): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.-363-1194dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238263 | |||||||
| chr3:119238263 | T | TAA | 14 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(11): Show |
21 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-363-1195_-363-119 others(6): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238263 | |||||||
| chr3:119238263 | TA | T | 6 | a0001c0001t0001g0126 a0001c0001t0002g0181 a0001c0003t0002g0198 others(3): Show |
6 | HG01081.hp1 HG01993.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-363-1194delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238263 | |||||||
| chr3:119238367 | C | T | 1 | a0002c0002t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-363-1297G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238367 | |||||||
| chr3:119238405 | T | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(8): Show |
20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-363-1335A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238405 | |||||||
| chr3:119238522 | C | T | 1 | a0001c0001t0002g0181 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-363-1452G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238522 | |||||||
| chr3:119238523 | G | A | 73 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0036 others(70): Show |
137 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.-363-1453C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238523 | |||||||
| chr3:119238643 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(8): Show |
20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-363-1573G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238643 | |||||||
| chr3:119238697 | C | A | 27 | a0001c0001t0002g0201 a0001c0001t0002g0210 a0001c0003t0002g0001 others(24): Show |
78 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-363-1627G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238697 | |||||||
| chr3:119238701 | G | A | 1 | a0001c0001t0002g0039 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-363-1631C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238701 | |||||||
| chr3:119238725 | C | T | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0115 others(9): Show |
20 | HG01433.hp2 HG01496.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-363-1655G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238725 | |||||||
| chr3:119238780 | C | T | 1 | a0002c0002t0001g0087 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-363-1710G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238780 | |||||||
| chr3:119238984 | C | T | 1 | a0001c0003t0002g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-364+1866G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119238984 | |||||||
| chr3:119239043 | A | G | 4 | a0001c0001t0003g0028 a0001c0001t0003g0145 a0001c0001t0003g0160 others(1): Show |
6 | HG02280.hp1 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-364+1807T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239043 | |||||||
| chr3:119239066 | A | T | 174 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(171): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-364+1784T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239066 | |||||||
| chr3:119239089 | T | A | 2 | a0001c0001t0002g0105 a0001c0001t0002g0106 |
2 | HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-364+1761A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239089 | |||||||
| chr3:119239248 | C | T | 1 | a0001c0009t0002g0093 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-364+1602G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239248 | |||||||
| chr3:119239325 | C | CA | 22 | a0001c0001t0001g0115 a0001c0001t0003g0003 a0001c0001t0003g0017 others(19): Show |
41 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.-364+1524dupT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239325 | |||||||
| chr3:119239325 | C | CAA | 41 | a0001c0001t0001g0024 a0001c0001t0001g0060 a0001c0001t0001g0094 others(38): Show |
57 | HG00544.hp1 HG00639.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.-364+1523_-364+152 others(6): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239325 | |||||||
| chr3:119239325 | C | CAAA | 67 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0092 others(64): Show |
135 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.-364+1522_-364+152 others(7): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239325 | |||||||
| chr3:119239325 | C | CAAAA | 34 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(31): Show |
63 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-364+1521_-364+152 others(8): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239325 | |||||||
| chr3:119239325 | C | CAAAAA | 12 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0107 others(9): Show |
20 | HG01070.hp1 HG01071.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.-364+1520_-364+152 others(9): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239325 | |||||||
| chr3:119239356 | G | A | 175 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(172): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-364+1494C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239356 | |||||||
| chr3:119239514 | T | G | 1 | a0001c0001t0012g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-364+1336A>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239514 | |||||||
| chr3:119239696 | T | A | 1 | a0001c0003t0002g0214 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-364+1154A>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239696 | |||||||
| chr3:119239759 | T | C | 1 | a0001c0001t0002g0181 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-364+1091A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239759 | |||||||
| chr3:119239772 | C | A | 62 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(59): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.-364+1078G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239772 | |||||||
| chr3:119239780 | C | G | 1 | a0001c0009t0002g0093 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-364+1070G>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239780 | |||||||
| chr3:119239838 | C | A | 11 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(8): Show |
20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-364+1012G>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239838 | |||||||
| chr3:119239852 | C | T | 1 | a0001c0001t0003g0142 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-364+998G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239852 | |||||||
| chr3:119239905 | G | T | 3 | a0001c0003t0002g0058 a0002c0002t0001g0056 a0002c0002t0001g0057 |
3 | NA18946.hp2 NA19006.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-364+945C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239905 | |||||||
| chr3:119239997 | TA | T | 85 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0024 others(82): Show |
159 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.-364+852delT | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239997 | |||||||
| chr3:119239997 | TAA | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0014 others(85): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-364+851_-364+852d others(4): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119239997 | |||||||
| chr3:119240000 | A | T | 1 | a0001c0001t0001g0138 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-364+850T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240000 | |||||||
| chr3:119240032 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0129 others(4): Show |
11 | HG01433.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-364+818C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240032 | |||||||
| chr3:119240044 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0052 others(8): Show |
28 | HG00408.hp1 HG02083.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.-364+806T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240044 | |||||||
| chr3:119240045 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0217 others(3): Show |
17 | HG00408.hp1 NA18943.hp1 NA18944.hp2 others(14): Show |
intron_variant | MODIFIER | c.-364+805A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240045 | |||||||
| chr3:119240071 | A | T | 23 | a0001c0001t0001g0014 a0001c0001t0001g0115 a0001c0001t0001g0126 others(20): Show |
40 | HG00609.hp2 HG00738.hp1 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.-364+779T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240071 | |||||||
| chr3:119240107 | G | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0133 a0001c0001t0001g0134 others(8): Show |
20 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-364+743C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240107 | |||||||
| chr3:119240193 | A | G | 21 | a0001c0001t0001g0014 a0001c0001t0001g0115 a0001c0001t0001g0126 others(18): Show |
38 | HG00609.hp2 HG00738.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.-364+657T>C | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240193 | |||||||
| chr3:119240202 | T | C | 1 | a0002c0002t0006g0034 | 2 | HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-364+648A>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240202 | |||||||
| chr3:119240222 | A | T | 1 | a0002c0002t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-364+628T>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240222 | |||||||
| chr3:119240241 | G | GT | 5 | a0001c0001t0002g0026 a0001c0001t0002g0039 a0001c0001t0002g0111 others(2): Show |
8 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.-364+608dupA | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240241 | |||||||
| chr3:119240363 | C | T | 76 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
142 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.-364+487G>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240363 | |||||||
| chr3:119240468 | A | C | 50 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0092 others(47): Show |
102 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.-364+382T>G | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240468 | |||||||
| chr3:119240757 | G | A | 1 | a0003c0006t0002g0053 | 2 | HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-364+93C>T | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240757 | |||||||
| chr3:119240823 | G | T | 1 | a0001c0005t0010g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-364+27C>A | B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1/7 | chr3 | 119240823 |